| Tag | Content |
|---|
EnhancerAtlas ID | HS049-01557 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr11:116298300-116299570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr11:116298457-116298468 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr11:116298456-116298467 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr11:116298457-116298467 | TCAAGGTCAT | + | 6.02 | | Gata4 | MA0482.1 | chr11:116299290-116299301 | GGGAGATAAGA | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63251 | chr11:116282793-116299761 | GLC16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I116426 | chr11 | 116297369 | 116300113 |
|
Enhancer Sequence | CTTGAGCTAA TGTGAGGGCC CAGGGATCTA GAATCCTATC TAAACCCCAG GCCTAACTAT 60
CCCTCAATTC TACAATGTCA TAGCTTGGGA GCCTAAAAGC TGGACAGAGT CGTCTCCTCT 120
GAAATGGCCT AGCCCCTGTC CTTTCAGAGA GAGCTTCTCA AGGTCATTGC AAAACCAGGC 180
TCTCAAGGCC CCTCCCTACA GCCTCGGCTT TCCTCTCTAG GAGCAAAGTC CCACCAAGAC 240
CTGAACTCTA GCTGCAAGAA TTCAAGACGT GTTCAATTCA CTTCCAGGTT CTCCTCCCAC 300
CCACCACCAG CCCTCTATCC CCCAGAGCTA GGCAGCAGCT GCTGTTAGGA GATCCTATCC 360
AGCCCTGGCT TGACATTTCA ACAGCCCGAG ACCCAGAGAT AAAAGTTGTC ACTGAACAAA 420
GTTCATCCCC CTCTCCCGCT CCCTTCCTGG AGCCTCGATA GGCATCAGAA TGGGCACTGA 480
GATGGTCTCT CTTGCTTTCT ACTGCTGCTG CCGCTGCTGC AATTCCTGCT TTTTATTTAG 540
AGGGGTGGGG GGAGATTTCA CAACTGATGA TTACGAAGAA GCGGTTTATC ACCTGTGCTT 600
TTATGATTGT AGCGACTAAG GGGAAAAAGA TGTCTTTTCA GATAAGCATT TGAAGGACGG 660
GGAGAAAGAT TTTCAAAGCT CCCTTTGTTC TCCTGGAGGG CCACGCCATT GAGTTCTGGC 720
AGGCAGCCCG GGAGAAAGGA GGATTTTAAA AACACAATCT GAGCTGGCTT CCAAACCCCT 780
GCTCACCATC CCTGTCATCA ATTAGGGATG TTACTTAACA AGGGGTTTGG GCCATTGTCT 840
CATCCAGCCT GCTTTCCCTA ATTGGATGCA GAGTGGTGAT GAATTATTTG GAAAAGGGCT 900
CCACACTGCA GAGGTCATTG CTTTGGCCCC CTGACACTCA AGGCCAGCTC AGGCTGGGCT 960
GGTGTGGGCC TCTGGGGCAT GTTGCTGGCA GGGAGATAAG AGAAGGACCT TTCTGAGGCC 1020
CCTCAGTGCA GGCGGAGAGC ACAGACCCAG AACCCAGAGA AGGGCAGGCT GCCAGTCCAT 1080
GCGGGGAACT GAAGGTGAGT GGCCAGGGAG AAGATGGGGG CCGCTCCTGT GGCCTCTGCC 1140
ACCCCCAGCC CCCACTCCAG TTTCTGAAGA TGGAGCTCGG TGAGCACAGA GAGCTTTAAG 1200
GCCTCAGTCC ACAAAGGGAC GGGTCTGAAT TCGTTAGGTC AAACTGCCAT AGACTCATAA 1260
ATATTGTGCC 1270
|
